HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → 2-(p-Chlorobenzylidene)-1-indanone oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(p-Chlorobenzylidene)-1-indanone | HCID 367217 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(p-Chlorobenzylidene)-1-indanone oxide | HCID 86736691 | — |
Reaction Steps
Ten grams (0.039 mole) of 2-(p-chlorobenzylidene)-1-indanone is converted to the epoxide in 1 liter of MeOH, using 9.6 g (0.085 mole) of 30% H2O2 and 9.6 ml (0.039 mole) of 16% NaOH, as described in Example 1. Since the starting material is poorly soluble in MeOH it is oxidized as a suspension and the product separates during the course of the reaction (5 hours at 35°-38°). The crude yield is 10 g (94%); m.p. 162°-164°. Crystallization (of 9.7 g) from 70 ml of MeCN gives 8.8 g (86%) of nearly colorless solid; m.p. 165°-167°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04173634 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-594ea544cd3e4ecf976a92c8aafa37d0 |
| Source note | uspto-grants-1979_11 |